Pain Clinic programs - anyone attended one of these?
Posted: Sun May 08, 2011 1:47 am
Has anyone been referred to a Pain Clinic for PN pain? I understand they are big in Australia.
I am so fed up with useless advice and treatments that often make me worse, so I want to check this out before wasting any time going there. I got a book from the library called Manage Your Pain by Dr. Michael Nicholas, who is big in Australia. The director of the Pain Clinic at my local hospital worked with him in Australia before opening the program here in Canada, so she's likely duplicating what they are doing in Sydney. They work with people who have any type of chronic pain, but its usually back or limb pain. Cognitive behaviour therapy sessions are a big part of the program. If these are group sessions, there is no way I would go - especially co-ed sessions (no offence fellows). I just can't imagine discussing my "private" pain with a bunch of people with back or limb pain!
One of their beliefs is that you can't make yourself worse by being more active or exercising as directed, even if the pain is worse. I'm not so sure that this is true for the pudendal nerve. I have read that the pudendal nerve has both sensory and motor functions, and is involved in controlling the muscles involved in urination and defecation. I got the impression that if I continued to ignore the agony and aggravated the nerve by sitting all day, I ran the risk of becoming incontinent. Anyone know if this is true?
I am so fed up with useless advice and treatments that often make me worse, so I want to check this out before wasting any time going there. I got a book from the library called Manage Your Pain by Dr. Michael Nicholas, who is big in Australia. The director of the Pain Clinic at my local hospital worked with him in Australia before opening the program here in Canada, so she's likely duplicating what they are doing in Sydney. They work with people who have any type of chronic pain, but its usually back or limb pain. Cognitive behaviour therapy sessions are a big part of the program. If these are group sessions, there is no way I would go - especially co-ed sessions (no offence fellows). I just can't imagine discussing my "private" pain with a bunch of people with back or limb pain!
One of their beliefs is that you can't make yourself worse by being more active or exercising as directed, even if the pain is worse. I'm not so sure that this is true for the pudendal nerve. I have read that the pudendal nerve has both sensory and motor functions, and is involved in controlling the muscles involved in urination and defecation. I got the impression that if I continued to ignore the agony and aggravated the nerve by sitting all day, I ran the risk of becoming incontinent. Anyone know if this is true?